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Cross-talk between myeloid-derived suppressor cells (MDSC), macrophages, and dendritic cells enhances tumor-induced immune suppression

Journal

SEMINARS IN CANCER BIOLOGY
Volume 22, Issue 4, Pages 275-281

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2012.01.011

Keywords

Tumor immunity; Immune escape; Tumor microenvironment; Tumor-associated macrophages

Categories

Funding

  1. NIH [RO1CA115880, RO1CA84232]
  2. American Cancer Society [IRG-97-153-07]
  3. DOD Breast Cancer Program [W81XWH-11-1-0115]

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The tumor microenvironment is a complex milieu of tumor and host cells. Host cells can include tumor-reactive T cells capable of killing tumor cells. However, more frequently the tumor and host components interact to generate a highly immune suppressive environment that frustrates T cell cytotoxicity and promotes tumor progression through a variety of immune and non-immune mechanisms. Myeloid-derived suppressor cells (MDSC) are a major host component contributing to the immune suppressive environment. In addition to their inherent immune suppressive function, MDSC amplify the immune suppressive activity of macrophages and dendritic cells via cross-talk This article will review the cell-cell interactions used by MDSC to inhibit anti-tumor immunity and promote progression, and the role of inflammation in promoting cross-talk between MDSC and other cells in the tumor microenvironment. (C) 2012 Published by Elsevier Ltd.

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